美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
45963-677-11	45963-677	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191210	N/A	ANDA	ANDA204161	Actavis Pharma, Inc.	METOPROLOL SUCCINATE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-677-11)
51655-934-52	51655-934	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220916	N/A	ANDA	ANDA204161	Northwind Pharmaceuticals, LLC	METOPROLOL SUCCINATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-934-52)
45963-677-96	45963-677	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191023	N/A	ANDA	ANDA204161	Actavis Pharma, Inc.	METOPROLOL SUCCINATE	100 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-677-96)
53002-2781-0	53002-2781	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	25 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2781-0)
53002-2781-3	53002-2781	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2781-3)